Allele Registry

Canonical Allele Identifier: PA2741950654

Gene: MED13L HGNC NCBI

ClinVar Allele:

2907272

ClinVar RCV:

RCV003497687

ClinVar Variation:

2745212

HGVS (amino-acid)	Matching Registered Transcripts
NP_056150.1:p.Asn158Asp	CA386926787 NM_015335.5:c.472A>G